Canonical Allele Identifier: CA2582342973

Gene: FGFR4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090796_177090800delinsTCTCA , CM000667.2:g.177090796_177090800delinsTCTCA	GRCh38
NC_000005.9:g.176517797_176517801delinsTCTCA , CM000667.1:g.176517797_176517801delinsTCTCA	GRCh37
NC_000005.8:g.176450403_176450407delinsTCTCA	NCBI36
NG_012067.1:g.8877_8881delinsTCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.407_411delinsTCTCA MANE Select	ENSP00000292408.4:p.Pro136Leu
ENST00000292408.8:c.407_411delinsTCTCA	ENSP00000292408.4:p.Pro136Leu
ENST00000393637.5:c.407_411delinsTCTCA	ENSP00000377254.1:p.Pro136Leu
ENST00000393648.6:c.407_411delinsTCTCA	ENSP00000377259.2:p.Pro136Leu
ENST00000426612.5:n.412_416delinsTCTCA
ENST00000430285.5:c.*271_*275delinsTCTCA	ENSP00000395164.1:n.*271_*275delinsTCTCA
ENST00000502906.5:c.407_411delinsTCTCA	ENSP00000424960.1:p.Pro136Leu
ENST00000503708.5:c.407_411delinsTCTCA	ENSP00000424905.1:p.Pro136Leu
ENST00000509511.5:n.407_411delinsTCTCA
NM_001291980.1:c.407_411delinsTCTCA	NP_001278909.1:p.Pro136Leu
NM_002011.4:c.407_411delinsTCTCA	NP_002002.3:p.Pro136Leu
NM_022963.3:c.407_411delinsTCTCA	NP_075252.2:p.Pro136Leu
NM_213647.2:c.407_411delinsTCTCA	NP_998812.1:p.Pro136Leu
XM_005265838.2:c.407_411delinsTCTCA	XP_005265895.1:p.Pro136Leu
XM_011534464.1:c.500_504delinsTCTCA	XP_011532766.1:p.Pro167Leu
XM_011534465.1:c.89_93delinsTCTCA	XP_011532767.1:p.Pro30Leu
XR_941090.1:n.452_456delinsTCTCA
NM_001354984.1:c.407_411delinsTCTCA	NP_001341913.1:p.Pro136Leu
NM_213647.3:c.407_411delinsTCTCA MANE Select	NP_998812.1:p.Pro136Leu
NM_001291980.2:c.407_411delinsTCTCA	NP_001278909.1:p.Pro136Leu
NM_001354984.2:c.407_411delinsTCTCA	NP_001341913.1:p.Pro136Leu
NM_002011.5:c.407_411delinsTCTCA	NP_002002.3:p.Pro136Leu